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1-Piperidineacetamide, N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72336-19-7

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72336-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72336-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72336-19:
(7*7)+(6*2)+(5*3)+(4*3)+(3*6)+(2*1)+(1*9)=117
117 % 10 = 7
So 72336-19-7 is a valid CAS Registry Number.

72336-19-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-piperidin-1-ylacetamide

1.2 Other means of identification

Product number -
Other names N-benzyl-2-piperidylacetamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72336-19-7 SDS

72336-19-7Downstream Products

72336-19-7Relevant academic research and scientific papers

Synthesis of an array of amides by aluminium chloride assisted cleavage of resin-bound esters

Barn, David R.,Morphy, J. Richard,Rees, David C.

, p. 3213 - 3216 (2007/10/03)

A new method for the synthesis of amino amides using Wang or Tentagel-PHB resins is described. The method uses aluminium chloride to promote the conversion of resin-bound benzylic esters to amides under ambient conditions. The reactions were monitored in 'real-time' using 13C gel phase NMR.

Quantitative structure-activity relationships for N-[(N',N'-disubstituted-amino)acetyl]arylamines for local anesthetic activity and acute toxicity

Heymans,Le Therizien,Godfroid,Bessin

, p. 184 - 193 (2007/10/02)

The synthesis and physicochemical properties of a series of N-[(N',N'-disubstituted-amino)acetyl]arylamines are described. A QSAR method is applied to local anesthetic activity and acute toxicity by means of a 'nonclassic' substituent variation involving a modification on both aryl and amino moieties. The choice of the different parameters (partition coefficient, pK(a), connectivity index, molar refraction, and molar volume) is discussed and their different methods of determination are described. Molar refraction is the parameter which explains best the variance of the local anesthetic activity, and the quadratic regression with MR leads to a 'a posteriori' synthesis of one compound with optimized activity. However, the partition coefficient is the most explicative parameter for intravenous toxicity.

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